TY - JOUR
T1 - Diffusion behavior of selenite in purified bentonite
AU - Idemitsu, Kazuya
AU - Kozaki, Hikaru
AU - Yuhara, Masaru
AU - Arima, Tatsumi
AU - Inagaki, Yaohiro
N1 - Funding Information:
This research is partly financed by a Grant-in-Aid for Scientific Research (grant number S24226021 ). Authors are indebted to Dr. Midori Watanabe, the Center of Advanced Instrumental Analysis, Kyushu University for the measurement of selenium concentration with ICP-MS. XANES measurements were performed with the approval of SAGA Light Source (Proposal No. 1304023R).
Publisher Copyright:
© 2015 Elsevier Ltd
Copyright:
Copyright 2016 Elsevier B.V., All rights reserved.
PY - 2016/9/1
Y1 - 2016/9/1
N2 - Selenium (Se) is an important element for assessing the safety of high-level waste disposal. In this study, the diffusion coefficients of selenite in purified bentonite were investigated. A Japanese purified sodium bentonite, Kunipia-F, which contains approximately 99 wt% montmorillonite, was used in this experiment. Bentonite powder was compacted into cylinders (diameter, 10 mm; height, 10 mm; dry density, 0.8–1.6 Mg m−3). Each compacted bentonite specimen was inserted into an acrylic resin column and saturated with 0.01 M–1.0 M of NaCl (aq.) for 30 days. One side of the bentonite was spiked with 10 μL of tracer solution containing 0.13 M Na2SeO3 and it was kept at 10, 25, 40, or 55 °C for 1–29 days. The apparent diffusion coefficients of selenite in compacted bentonite were 2.5 × 10−11 to 1.9 × 10−13 m2 s−1 and decreased with the increase in dry density. The ionic strength showed no significant effect on the apparent diffusion coefficient of selenite for bentonite densities higher than 1.4 Mg m−3. However, the apparent diffusion coefficients for 1 M NaCl were several times larger than those in 0.1 or 0.01 M NaCl for densities lower than 1.2 Mg m−3. This increase in diffusion coefficient would be caused by a change in anion accessible porosity. The apparent diffusion coefficient would be explained by Archie's law and is proportional to exponentiation of porosity. It is desired to measure exact anion accessible porosity. The activation energy of selenite in purified bentonite was 20 ± 4 kJ mol−1 and was similar to the activation energies of oxo-anions in free water. This also indicates that selenite diffuses in free pore water in the bentonite.
AB - Selenium (Se) is an important element for assessing the safety of high-level waste disposal. In this study, the diffusion coefficients of selenite in purified bentonite were investigated. A Japanese purified sodium bentonite, Kunipia-F, which contains approximately 99 wt% montmorillonite, was used in this experiment. Bentonite powder was compacted into cylinders (diameter, 10 mm; height, 10 mm; dry density, 0.8–1.6 Mg m−3). Each compacted bentonite specimen was inserted into an acrylic resin column and saturated with 0.01 M–1.0 M of NaCl (aq.) for 30 days. One side of the bentonite was spiked with 10 μL of tracer solution containing 0.13 M Na2SeO3 and it was kept at 10, 25, 40, or 55 °C for 1–29 days. The apparent diffusion coefficients of selenite in compacted bentonite were 2.5 × 10−11 to 1.9 × 10−13 m2 s−1 and decreased with the increase in dry density. The ionic strength showed no significant effect on the apparent diffusion coefficient of selenite for bentonite densities higher than 1.4 Mg m−3. However, the apparent diffusion coefficients for 1 M NaCl were several times larger than those in 0.1 or 0.01 M NaCl for densities lower than 1.2 Mg m−3. This increase in diffusion coefficient would be caused by a change in anion accessible porosity. The apparent diffusion coefficient would be explained by Archie's law and is proportional to exponentiation of porosity. It is desired to measure exact anion accessible porosity. The activation energy of selenite in purified bentonite was 20 ± 4 kJ mol−1 and was similar to the activation energies of oxo-anions in free water. This also indicates that selenite diffuses in free pore water in the bentonite.
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U2 - 10.1016/j.pnucene.2015.08.012
DO - 10.1016/j.pnucene.2015.08.012
M3 - Article
AN - SCOPUS:84940850359
SN - 0149-1970
VL - 92
SP - 279
EP - 285
JO - Progress in Nuclear Energy
JF - Progress in Nuclear Energy
ER -